SA06270491B1 - تركيبة مبيدة للأعشاب تشتمل على حمض 2، 2- ثنائي ميثيل بروبيونيك 8- (2، 6- ثنائي إيثيل –4- ميثيل – فينيل) –9- أوكسو –1، 2، 4، 5- تتراهيدرو –9h- بيرازولو[2.1-دي][ 5.4.1] أوكسادايازيبين –7- يل إستر وكحول - Google Patents

تركيبة مبيدة للأعشاب تشتمل على حمض 2، 2- ثنائي ميثيل بروبيونيك 8- (2، 6- ثنائي إيثيل –4- ميثيل – فينيل) –9- أوكسو –1، 2، 4، 5- تتراهيدرو –9h- بيرازولو[2.1-دي][ 5.4.1] أوكسادايازيبين –7- يل إستر وكحول Download PDF

Info

Publication number: SA06270491B1
Authority: SA; Saudi Arabia
Prior art keywords: alcohol; diethyl; ester; pyrazolo; tetrahydro
Prior art date: 2005-12-27

Application number

SA6270491A

Other languages

Arabic (ar)

English (en)

Inventor

رودولف شنيدر

Original Assignee

سينجنتا بارتيسبيشنز ايه جي

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2005-12-27

Filing date

2006-12-24

Publication date

2010-10-20

2006-12-24 Application filed by سينجنتا بارتيسبيشنز ايه جي filed Critical سينجنتا بارتيسبيشنز ايه جي

2010-10-20 Publication of SA06270491B1 publication Critical patent/SA06270491B1/ar

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IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 title claims abstract description 23
230000002363 herbicidal effect Effects 0.000 title claims abstract description 22
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 15
-1 [1,4,5]Oxadiazepin-7-yl Chemical group 0.000 title claims abstract description 13
239000000203 mixture Substances 0.000 claims abstract description 39
239000004495 emulsifiable concentrate Substances 0.000 claims abstract description 18
239000004009 herbicide Substances 0.000 claims abstract description 18
238000009472 formulation Methods 0.000 claims abstract description 15
239000002904 solvent Substances 0.000 claims abstract description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 7
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims description 8
239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 8
COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical group C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 claims description 8
BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 claims description 8
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OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims description 2
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WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 claims 1
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OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 2
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150000004702 methyl esters Chemical class 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
RYDICHIKLKVOEJ-UHFFFAOYSA-N oxadiazepine Chemical compound O1C=CC=CN=N1 RYDICHIKLKVOEJ-UHFFFAOYSA-N 0.000 description 1
CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Polymers 0.000 description 1
MGOHCFMYLBAPRN-UHFFFAOYSA-N pinoxaden Chemical compound CCC1=CC(C)=CC(CC)=C1C(C1=O)=C(OC(=O)C(C)(C)C)N2N1CCOCC2 MGOHCFMYLBAPRN-UHFFFAOYSA-N 0.000 description 1
230000005080 plant death Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 description 1
BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
PZTAGFCBNDBBFZ-UHFFFAOYSA-N tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1CO PZTAGFCBNDBBFZ-UHFFFAOYSA-N 0.000 description 1
LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
FHYUCVWDMABHHH-UHFFFAOYSA-N toluene;1,2-xylene Chemical compound CC1=CC=CC=C1.CC1=CC=CC=C1C FHYUCVWDMABHHH-UHFFFAOYSA-N 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000003799 water insoluble solvent Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Zoology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

SA6270491A 2005-12-27 2006-12-24 تركيبة مبيدة للأعشاب تشتمل على حمض 2، 2- ثنائي ميثيل بروبيونيك 8- (2، 6- ثنائي إيثيل –4- ميثيل – فينيل) –9- أوكسو –1، 2، 4، 5- تتراهيدرو –9h- بيرازولو[2.1-دي][ 5.4.1] أوكسادايازيبين –7- يل إستر وكحول SA06270491B1 (ar)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH20752005		2005-12-27

Publications (1)

Publication Number	Publication Date
SA06270491B1 true SA06270491B1 (ar)	2010-10-20

Family

ID=38080896

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SA6270491A SA06270491B1 (ar)	2005-12-27	2006-12-24	تركيبة مبيدة للأعشاب تشتمل على حمض 2، 2- ثنائي ميثيل بروبيونيك 8- (2، 6- ثنائي إيثيل –4- ميثيل – فينيل) –9- أوكسو –1، 2، 4، 5- تتراهيدرو –9h- بيرازولو[2.1-دي][ 5.4.1] أوكسادايازيبين –7- يل إستر وكحول

Country Status (22)

Country	Link
US (3)	US10952437B2 (de)
EP (1)	EP1965646B1 (de)
JP (1)	JP5086272B2 (de)
CN (1)	CN101453894B (de)
AR (1)	AR058747A1 (de)
AT (1)	ATE460839T1 (de)
AU (1)	AU2006331031B2 (de)
BR (1)	BRPI0621268B1 (de)
CA (1)	CA2632323C (de)
DE (1)	DE602006013038D1 (de)
DK (1)	DK1965646T3 (de)
EA (1)	EA018654B1 (de)
ES (1)	ES2341891T3 (de)
MA (1)	MA30087B1 (de)
PL (1)	PL1965646T3 (de)
PT (1)	PT1965646E (de)
SA (1)	SA06270491B1 (de)
SI (1)	SI1965646T1 (de)
TN (1)	TNSN08282A1 (de)
UA (1)	UA92512C2 (de)
WO (1)	WO2007073933A2 (de)
ZA (1)	ZA200804764B (de)

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CN105580820A (zh) *	2016-02-24	2016-05-18	陕西上格之路生物科学有限公司	一种含三甲苯草酮和唑啉草酯的除草组合物
EP3484288B1 (de)	2016-07-12	2024-11-27	Monsanto Technology LLC	Pestizidzusammensetzungen
CN106538558B (zh) *	2016-10-13	2018-10-16	北京明德立达农业科技有限公司	一种除草剂组合物及其应用
AU2018209803B2 (en) *	2017-01-23	2023-09-21	Syngenta Crop Protection Ag	Method of controlling weeds in warm season turfgrass
CN109757478A (zh) *	2017-11-09	2019-05-17	山东润博生物科技有限公司	一种麦草畏型乳油及其制备方法
KR102064661B1 (ko) *	2018-03-14	2020-01-09	장인국	적화용 조성물 및 이를 이용한 적화 방법
PL3950665T3 (pl)	2019-04-01	2024-04-02	Oriental (Luzhou) Agrochemicals. Co., Ltd.	Sprzężony związek trienowy, sposób jego wytwarzania i jego zastosowanie
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CN114554845B (zh) *	2019-07-18	2024-06-18	安道麦阿甘有限公司	包含除草剂的稳定制剂
CN114126407A (zh) *	2019-07-23	2022-03-01	江苏龙灯化学有限公司	乳油配制品及其用途
IL297035A (en)	2020-04-06	2022-12-01	Adama Agan Ltd	Co-crystals of antioxidants and active ingredients and use of antioxidants as stabilizer
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2006
- 2006-12-24 SA SA6270491A patent/SA06270491B1/ar unknown
- 2006-12-26 AR ARP060105792A patent/AR058747A1/es active IP Right Grant
- 2006-12-27 PT PT06841168T patent/PT1965646E/pt unknown
- 2006-12-27 PL PL06841168T patent/PL1965646T3/pl unknown
- 2006-12-27 CN CN2006800494363A patent/CN101453894B/zh active Active
- 2006-12-27 DK DK06841168.5T patent/DK1965646T3/da active
- 2006-12-27 JP JP2008547895A patent/JP5086272B2/ja active Active
- 2006-12-27 CA CA2632323A patent/CA2632323C/en active Active
- 2006-12-27 BR BRPI0621268A patent/BRPI0621268B1/pt active IP Right Grant
- 2006-12-27 WO PCT/EP2006/012539 patent/WO2007073933A2/en not_active Ceased
- 2006-12-27 UA UAA200809541A patent/UA92512C2/ru unknown
- 2006-12-27 AT AT06841168T patent/ATE460839T1/de active
- 2006-12-27 EP EP06841168A patent/EP1965646B1/de active Active
- 2006-12-27 DE DE602006013038T patent/DE602006013038D1/de active Active
- 2006-12-27 AU AU2006331031A patent/AU2006331031B2/en active Active
- 2006-12-27 SI SI200630652T patent/SI1965646T1/sl unknown
- 2006-12-27 US US12/159,138 patent/US10952437B2/en active Active
- 2006-12-27 EA EA200801448A patent/EA018654B1/ru not_active IP Right Cessation
- 2006-12-27 ES ES06841168T patent/ES2341891T3/es active Active
2008
- 2008-06-02 ZA ZA200804764A patent/ZA200804764B/xx unknown
- 2008-06-23 TN TNP2008000282A patent/TNSN08282A1/en unknown
- 2008-06-26 MA MA31077A patent/MA30087B1/fr unknown
2021
- 2021-03-16 US US17/202,997 patent/US20210195901A1/en active Pending
2023
- 2023-03-10 US US18/181,958 patent/US20230263163A1/en active Pending

Also Published As

Publication number	Publication date
JP5086272B2 (ja)	2012-11-28
AU2006331031B2 (en)	2013-06-13
PT1965646E (pt)	2010-05-20
DK1965646T3 (da)	2010-06-07
WO2007073933A3 (en)	2009-02-19
EA018654B1 (ru)	2013-09-30
SI1965646T1 (sl)	2010-07-30
CN101453894B (zh)	2012-08-08
US20230263163A1 (en)	2023-08-24
ES2341891T3 (es)	2010-06-29
CA2632323C (en)	2015-03-17
AU2006331031A1 (en)	2007-07-05
UA92512C2 (ru)	2010-11-10
US20090005246A1 (en)	2009-01-01
PL1965646T3 (pl)	2010-08-31
US20210195901A1 (en)	2021-07-01
WO2007073933A8 (en)	2008-07-17
ATE460839T1 (de)	2010-04-15
CA2632323A1 (en)	2007-07-05
EP1965646A2 (de)	2008-09-10
JP2009524597A (ja)	2009-07-02
DE602006013038D1 (de)	2010-04-29
ZA200804764B (en)	2009-10-28
WO2007073933A2 (en)	2007-07-05
TNSN08282A1 (en)	2009-10-30
BRPI0621268B1 (pt)	2015-10-27
EP1965646B1 (de)	2010-03-17
CN101453894A (zh)	2009-06-10
EA200801448A1 (ru)	2009-06-30
AR058747A1 (es)	2008-02-20
US10952437B2 (en)	2021-03-23
BRPI0621268A2 (pt)	2011-12-06
MA30087B1 (fr)	2008-12-01

Publication	Publication Date	Title
EP1965646B1 (de)	2010-03-17	Herbizide zusammensetzung
RU2637524C2 (ru)	2017-12-05	Жидкие агрохимические композиции, содержащие полимерный загуститель и спиртосодержащую систему растворителей, и жидкие гербицидные композиции, содержащие спиртосодержащую систему растворителей
EP2034836B1 (de)	2009-11-04	Hochfeste und niedrigtemperaturstabile herbizid-formulierungen aus fluorxypyrestern
AU704539B2 (en)	1999-04-29	Herbicides with 4-iodo-2-(3-(4-methoxy-6-methyl-1,3, 5-triazin-2-yl)urei dosulfonyl)-benzoic acid esters
EA023452B1 (ru)	2016-06-30	Гербицидные композиции, содержащие топрамезон, пиноксаден и клохинтоцет
KR20150096448A (ko)	2015-08-24	페녹스술람 및 메페나세트의 적용에 의한 상승작용적 잡초 방제
US20080153706A1 (en)	2008-06-26	Water-In-Oil Suspoemulsions
US20050064004A1 (en)	2005-03-24	Surfactant/solvent mixtures
HK1212861A1 (zh)	2016-06-24	來自施用環丙嘧啶酸和氯氨吡啶酸的協同雜草控制
EP1802195A1 (de)	2007-07-04	Tensid/lösungsmittelgemische
WO2008006456A1 (en)	2008-01-17	Herbicidal composition
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